Naphthodithiophene-2,1,3-benzothiadiazole copolymers for bulk heterojunction solar cells

被引:49
|
作者
Wang, Bao [2 ,3 ,4 ]
Tsang, Sai-Wing [1 ]
Zhang, Weifeng [2 ,3 ,4 ]
Tao, Ye [1 ]
Wong, Man Shing [2 ,3 ,4 ]
机构
[1] Natl Res Council Canada NRC, Inst Microstruct Sci IMS, Ottawa, ON K1A 0R6, Canada
[2] Hong Kong Baptist Univ, Inst Mol Funct Mat, Kowloon Tong, Hong Kong, Peoples R China
[3] Hong Kong Baptist Univ, Dept Chem, Kowloon Tong, Hong Kong, Peoples R China
[4] Hong Kong Baptist Univ, Ctr Adv Luminescence Mat, Kowloon Tong, Hong Kong, Peoples R China
关键词
EFFICIENCY; POLYMERS; BENZOTHIADIAZOLE; PERFORMANCE; MORPHOLOGY;
D O I
10.1039/c1cc13690a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two newly synthesized naphthodithiophene-based copolymers, PNB, exhibit a low optical bandgap of similar to 1.64 eV with which the solar cells fabricated from the blend of PNB and PC71BM afforded a power conversion efficiency of 5.3% with external quantum efficiency over 60% in a broad spectral range.
引用
收藏
页码:9471 / 9473
页数:3
相关论文
共 50 条
  • [31] 2,1,3-Benzothiadiazole: Study of its structure, energetics and aromaticity
    Miranda, Margarida S.
    Matos, M. Agostinha R.
    Morais, Victor M. F.
    Liebman, Joel F.
    JOURNAL OF CHEMICAL THERMODYNAMICS, 2012, 50 : 30 - 36
  • [32] Thermodynamics of the intermolecular and intramolecular bonds in a molecule of 2,1,3-benzothiadiazole
    Sabbah, R
    Kuakuvi, DN
    Perez, L
    THERMOCHIMICA ACTA, 1998, 316 (02) : 137 - 143
  • [33] EPR-SPECTRA OF PHOSPHORESCENT STATE OF 2,1,3-BENZOTHIADIAZOLE
    LIN, TS
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1975, 170 (AUG24): : 34 - 34
  • [34] Intramolecular halogen bonding of 2,1,3-benzothiadiazole containing molecules
    Mancheski, Lucas
    Giebel, Sierra
    Speetzen, Erin
    Bosch, Eric
    Bowling, Nathan
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2017, 253
  • [36] Benzothiadiazole with π-Spacer as Efficient Chromophore for Bulk Heterojunction Organic Solar Cells
    Fijahi, Lamiaa
    Ameen, Sadia
    Akhtar, M. Shaheer
    Abdullah
    Kim, Eun-Bi
    Kim, Tae-Geum
    Shin, Hyung-Shik
    NANOSCIENCE AND NANOTECHNOLOGY LETTERS, 2019, 11 (02) : 151 - 158
  • [37] Synthesis and Characterization of Copolymers with Fluorene-di-2-thienyl-2,1,3-benzothiadiazole Units for Application in Optoelectronic Devices
    de Brito, Elisa Barbosa
    Santos, Daniela Correa
    de Paula, Taihana Parente
    de Morais, Andreia
    de Freitas, Jilian Nei
    Marques, Maria de Fatima Vieira
    Monteiro, Sergio Neves
    POLYMERS, 2025, 17 (01)
  • [38] ROTATIONAL BAND CONTOURS IN 3280 A ELECTRONIC SYSTEM OF 2,1,3-BENZOTHIADIAZOLE
    CHRISTOFFERSEN, J
    HOLLAS, JM
    WRIGHT, RA
    PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1969, 308 (1495) : 537 - +
  • [39] Chemodosimeters for mercury(II) and methylmercury(I) based on 2,1,3-benzothiadiazole
    Zou, Qi
    Tian, He
    SENSORS AND ACTUATORS B-CHEMICAL, 2010, 149 (01): : 20 - 27
  • [40] Hyperconjugated side chained benzodithiophene and 4,7-di-2-thienyl-2,1,3-benzothiadiazole based polymer for solar cells
    Liu, Qian
    Bao, Xichang
    Wen, Shuguang
    Du, Zhengkun
    Han, Liangliang
    Zhu, Dangqiang
    Chen, Yanhua
    Sun, Mingliang
    Yang, Renqiang
    POLYMER CHEMISTRY, 2014, 5 (06) : 2076 - 2082